The role of TREM2 in Alzheimer's disease and other neurodegenerative disorders von Carmona, Susana, Zahs, Kathleen, Wu, Elizabeth, Dakin, Kelly, Bras, Jose, Guerreiro, Rita

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The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE von Guerreiro, Rita J, Gustafson, Deborah R, Hardy, John

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Reply to: Genome-wide association studies of polygenic risk score-derived phenotypes may lead to inflated false positive rates von Guerreiro, Rita, Bras, Jose

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Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis von BRAS, Jose, VERLOES, Alain, SCHNEIDER, Susanne A, MOLE, Sara E, GUERREIRO, Rita J

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A Paired RNAi and RabGAP Overexpression Screen Identifies Rab11 as a Regulator of β-Amyloid Production von Udayar, Vinod, Buggia-Prévot, Virginie, Guerreiro, Rita L., Siegel, Gabriele, Rambabu, Naresh, Soohoo, Amanda L., Ponnusamy, Moorthi, Siegenthaler, Barbara, Bali, Jitin, Guerreiro, Rita, Brás, José, Sassi, Celeste, Gibbs, J. Raphael, Hernandez, Dena, Lupton, Michelle K., Brown, Kristelle, Morgan, Kevin, Powell, John, Singleton, Andrew, Hardy, John, Simons, Mikael, Ries, Jonas, Puthenveedu, Manojkumar A., Hardy, John, Thinakaran, Gopal, Rajendran, Lawrence

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Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series von Ryan, Natalie S, Dr, Nicholas, Jennifer M, PhD, Weston, Philip S J, MRCP, Liang, Yuying, MRCP, Lashley, Tammaryn, PhD, Guerreiro, Rita, PhD, Adamson, Gary, BSc, Kenny, Janna, MRCP, Beck, Jon, FRCPath, Chavez-Gutierrez, Lucia, PhD, de Strooper, Bart, Prof, Revesz, Tamas, Prof, Holton, Janice, Prof, Mead, Simon, Prof, Rossor, Martin N, Prof, Fox, Nick C, Prof

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A locked immunometabolic switch underlies TREM2 R47H loss of function in human iPSC‐derived microglia von Piers, Thomas M., Cosker, Katharina, Mallach, Anna, Johnson, Gabriel Thomas, Guerreiro, Rita, Hardy, John, Pocock, Jennifer M.

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Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia–like Syndrome Without Bone Involvement von Guerreiro, Rita João, Lohmann, Ebba, Brás, José Miguel, Gibbs, Jesse Raphael, Rohrer, Jonathan D, Gurunlian, Nicole, Dursun, Burcu, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Emre, Murat, Singleton, Andrew, Hardy, John

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Challenge accepted: uncovering the role of rare genetic variants in Alzheimer's disease von Khani, Marzieh, Gibbons, Elizabeth, Bras, Jose, Guerreiro, Rita

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Genome-wide association of polygenic risk extremes for Alzheimer's disease in the UK Biobank von Gouveia, Catarina, Gibbons, Elizabeth, Dehghani, Nadia, Eapen, James, Guerreiro, Rita, Bras, Jose

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Use of next-generation sequencing and other whole-genome strategies to dissect neurological disease von Bras, Jose, Guerreiro, Rita, Hardy, John

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A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD von Renton, Alan E., Majounie, Elisa, Waite, Adrian, Simón-Sánchez, Javier, Rollinson, Sara, Gibbs, J. Raphael, Schymick, Jennifer C., Laaksovirta, Hannu, van Swieten, John C., Myllykangas, Liisa, Kalimo, Hannu, Paetau, Anders, Abramzon, Yevgeniya, Remes, Anne M., Kaganovich, Alice, Scholz, Sonja W., Duckworth, Jamie, Ding, Jinhui, Harmer, Daniel W., Hernandez, Dena G., Johnson, Janel O., Mok, Kin, Ryten, Mina, Trabzuni, Danyah, Guerreiro, Rita J., Orrell, Richard W., Neal, James, Murray, Alex, Pearson, Justin, Jansen, Iris E., Sondervan, David, Seelaar, Harro, Blake, Derek, Young, Kate, Halliwell, Nicola, Callister, Janis Bennion, Toulson, Greg, Richardson, Anna, Gerhard, Alex, Snowden, Julie, Mann, David, Neary, David, Nalls, Michael A., Peuralinna, Terhi, Jansson, Lilja, Isoviita, Veli-Matti, Kaivorinne, Anna-Lotta, Hölttä-Vuori, Maarit, Ikonen, Elina, Sulkava, Raimo, Benatar, Michael, Wuu, Joanne, Chiò, Adriano, Restagno, Gabriella, Borghero, Giuseppe, Sabatelli, Mario, Heckerman, David, Rogaeva, Ekaterina, Zinman, Lorne, Rothstein, Jeffrey D., Sendtner, Michael, Drepper, Carsten, Eichler, Evan E., Alkan, Can, Abdullaev, Ziedulla, Pack, Svetlana D., Dutra, Amalia, Pak, Evgenia, Hardy, John, Singleton, Andrew, Williams, Nigel M., Heutink, Peter, Pickering-Brown, Stuart, Morris, Huw R., Tienari, Pentti J., Traynor, Bryan J.

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Genetic architecture of common non-Alzheimer’s disease dementias von Guerreiro, Rita, Gibbons, Elizabeth, Tábuas-Pereira, Miguel, Kun-Rodrigues, Celia, Santo, Gustavo C., Bras, Jose

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Correction: Challenge accepted: Uncovering the role of rare genetic variants in Alzheimer’s disease von Khani, Marzieh, Gibbons, Elizabeth, Bras, Jose, Guerreiro, Rita

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Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease von Neumann, Juliane, Bras, Jose, Deas, Emma, O'Sullivan, Sean S., Parkkinen, Laura, Lachmann, Robin H., Li, Abi, Holton, Janice, Guerreiro, Rita, Paudel, Reema, Segarane, Badmavady, Singleton, Andrew, Lees, Andrew, Hardy, John, Houlden, Henry, Revesz, Tamas, Wood, Nicholas W.

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The age factor in Alzheimer's disease von Guerreiro, Rita, Bras, Jose

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H-ABC syndrome and DYT4: Variable expressivity or pleiotropy of TUBB4 mutations? von Erro, Roberto, Hersheson, Joshua, Ganos, Christos, Mencacci, Niccoló E., Stamelou, Maria, Batla, Amit, Thust, Stefanie Catherine, Bras, Jose M., Guerreiro, Rita J., Hardy, John, Quinn, Niall P., Houlden, Henry, Bhatia, Kailash P.

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Genetics of Alzheimer’s Disease von Guerreiro, Rita, Hardy, John

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The Chihuahua dog: A new animal model for neuronal ceroid lipofuscinosis CLN7 disease? von Faller, Kiterie M.E., Bras, Jose, Sharpe, Samuel J., Anderson, Glenn W., Darwent, Lee, Kun-Rodrigues, Celia, Alroy, Joseph, Penderis, Jacques, Mole, Sara E., Gutierrez-Quintana, Rodrigo, Guerreiro, Rita J.

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Reconsidering the role of blood-brain barrier in Alzheimer's disease: From delivery to target von Sousa, João André, Bernardes, Catarina, Bernardo-Castro, Sara, Lino, Miguel, Albino, Inês, Ferreira, Lino, Brás, José, Guerreiro, Rita, Tábuas-Pereira, Miguel, Baldeiras, Inês, Santana, Isabel, Sargento-Freitas, João

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